CONVENTIONAL APPROACHES often don't lower triglycerides to guideline-recommended levels1–4

With conventional triglyceride-lowering approaches (e.g., statins, fibrates, and omega-3 fatty acids), people with Familial Chylomicronaemia Syndrome (FCS) still face a high risk of acute pancreatitis1–4

A strict, low-fat diet is the cornerstone of treatment in FCS5

Current FCS management primarily includes the use of an extremely low-fat diet (20–25 g/day) and avoidance of alcohol to manage high triglycerides.6 This remains essential for managing FCS symptoms and reducing the risk of acute pancreatitis, especially as conventional approaches show limited efficacy6

Despite this, in a survey of 166 people with FCS, participants reported the following regarding their restrictive diet:7

81%

reported it as extremely time consuming

70%

reported it as energy draining

53%

reported it as ineffective at stopping all symptoms

Man in a grey henley shirt and blue jeans standing with a slight lean, hands relaxed by his sides.

Not an actual patient

Targeted treatment is an option for people with FCS1,2,9

Conventional triglyceride-lowering approaches are focused on increasing lipoprotein lipase activity. However, given the lack of functional lipoprotein lipase activity in people with FCS, increased apolipoprotein C-III levels primarily lead to further increased triglyceride levels via lipoprotein lipase-independent pathways7,10

As a result, most people do not achieve the guideline-recommended triglyceride target of ≤10 mmol/L (880 mg/dL), leaving them at high risk of acute pancreatitis3,4,7,9

Apolipoprotein C-III is a recognised target for specialist therapies aiming to lower triglycerides in people with FCS. Volanesorsen is an EU-approved antisense oligonucleotide that targets hepatic apolipoprotein C-III mRNA2,11,12

How could achieving the guideline-recommended triglyceride target benefit people with FCS?

Find out more

Abbreviations

AP, acute pancreatitis; FCS, Familial Chylomicronaemia Syndrome.

Show References Expand Collapse

  1. Paragh G, Németh Á, et al. Lipids Health Dis. 2022;21:21.
  2. Spagnuolo CM, Hegele RA, et al. Expert Rev Endocrinol Metab. 2024;19(4):299–306.
  3. Gouni-Berthold I. J Endocr Soc. 2020;4(2):bvz037.
  4. Mach F, Baigent C, et al. Eur Heart J. 2020;41(1):111–88.
  5. Shamsudeen I, Hegele RA, et al. Expert Rev Clin Pharmacol. 2022;15(4):395–405.
  6. Stroes E, Moulin P, et al. Atheroscler Suppl. 2017;23:1–7.
  7. Davidson M, Stevenson M, et al. J Clin Lipidol. 2018;12(4):898–907.
  8. Veliadkis N, Stachteas P, et al. Pharmaceuticals (Basel). 2024;17(5):568.
  9. Wolska A, Yang ZH, et al. Curr Opin Lipidol. 2020;31(6):331–9.
  10. Witztum JL, Tsimikas S, et al. J Clin Lipidol. 2023;17(3):342–55
  11. Goldberg RB, Chait A, et al. Front Endocrinol (Lausanne). 2020 Oct 23;11:593931.
  12. Larouche MB, Watts GF, et al. Curr Opin Endocrinol Diabetes Obes. 2025;32(2):75–88.

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